510(k) K090644
K090644 is an FDA 510(k) premarket notification submitted by Vita Zahnfabrik H.Rauter GmbH & Co. for the device "VITABLOCS, MODEL VX55-****". The FDA issued a decision of Substantially Equivalent on Mar 31, 2009. The device falls under product code EIH (Powder, Porcelain), a Class II device regulated under 21 CFR 872.6660. Vita Zahnfabrik H.Rauter GmbH & Co. has at least 5 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Mar 31, 2009
- Date Received
- Mar 10, 2009
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Powder, Porcelain
- Device Class
- Class II
- Regulation Number
- 872.6660
- Review Panel
- DE
- Submission Type